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      Crossed Pathways for Radiation-Induced and Immunotherapy-Related Lung Injury

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          Abstract

          Radiation-induced lung injury (RILI) is a form of radiation damage to normal lung tissue caused by radiotherapy (RT) for thoracic cancers, which is most commonly comprised of radiation pneumonitis (RP) and radiation pulmonary fibrosis (RPF). Moreover, with the widespread utilization of immunotherapies such as immune checkpoint inhibitors as first- and second-line treatments for various cancers, the incidence of immunotherapy-related lung injury (IRLI), a severe immune-related adverse event (irAE), has rapidly increased. To date, we know relatively little about the underlying mechanisms and signaling pathways of these complications. A better understanding of the signaling pathways may facilitate the prevention of lung injury and exploration of potential therapeutic targets. Therefore, this review provides an overview of the signaling pathways of RILI and IRLI and focuses on their crosstalk in diverse signaling pathways as well as on possible mechanisms of adverse events resulting from combined radiotherapy and immunotherapy. Furthermore, this review proposes potential therapeutic targets and avenues of further research based on signaling pathways. Many new studies on pyroptosis have renewed appreciation for the value and importance of pyroptosis in lung injury. Therefore, the authors posit that pyroptosis may be the common downstream pathway of RILI and IRLI; discussion is also conducted regarding further perspectives on pyroptosis as a crucial signaling pathway in lung injury treatment.

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          Most cited references210

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          Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018

          Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field.
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            Effective treatment of severe COVID-19 patients with tocilizumab

            Significance In patients with coronavirus disease 2019, a large number of T lymphocytes and mononuclear macrophages are activated, producing cytokines such as interleukin-6 (IL-6), which bind to the IL-6 receptor on the target cells, causing the cytokine storm and severe inflammatory responses in lungs and other tissues and organs. Tocilizumab, as a recombinant humanized anti-human IL-6 receptor monoclonal antibody, can bind to the IL-6 receptor with high affinity, thus preventing IL-6 itself from binding to its receptor, rendering it incapable of immune damage to target cells, and alleviating the inflammatory responses.
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              Immune-Related Adverse Events Associated with Immune Checkpoint Blockade

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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                01 December 2021
                2021
                01 December 2021
                : 12
                : 774807
                Affiliations
                [1] 1 Department of Radiation Oncology, Cheeloo College of Medicine, Shandong University , Jinan, China
                [2] 2 Department of Radiation Oncology, Laboratory of Radio-Immunology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences , Jinan, China
                [3] 3 Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center , Houston, TX, United States
                Author notes

                Edited by: Feng-Ming (Spring) Kong, The University of Hong Kong, Hong Kong SAR, China

                Reviewed by: Zhongxing Liao, University of Texas MD Anderson Cancer Center, United States; Rachel Evans, King’s College London, United Kingdom

                *Correspondence: Dawei Chen, dave0505@ 123456yeah.net ; Jinming Yu, sdyujinming@ 123456126.com

                This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology

                †These authors have contributed equally to this work and share first authorship

                Article
                10.3389/fimmu.2021.774807
                8672113
                34925345
                708d9c54-b0b5-44bc-bb06-a532129c5864
                Copyright © 2021 Zhang, Zhou, Verma, Liu, Wu, Yu and Chen

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 13 September 2021
                : 11 November 2021
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 210, Pages: 17, Words: 7253
                Categories
                Immunology
                Review

                Immunology
                radiation-induced lung injury,immunotherapy-related lung injury,immune checkpoint inhibitor,signaling pathway,pyroptosis

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